Product Details

SNP ID: rs149728406
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.8:23191916 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GGCCTGCTGTACCAGCTCTGACCAC[A/G]TCGATCTCATTTTTCGTGAGGTCCA
Phenotype: MIM: 603611
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: TNFRSF10A PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003844.3	1291	Silent Mutation	GAC,GAT	D395D	NP_003835.3